rs1799883, FABP2

N. diseases: 36
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2017 2017
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2007 2007
Carotid Stenosis
CUI: C0007282
Disease: Carotid Stenosis
19 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1 2007 2007
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2007 2007
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2009 2009
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2013 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 1998 1998
Familial hypercholesterolemia - heterozygous
34 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2004 2004
Gerstmann-Straussler-Scheinker Disease
39 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2016 2016
hearing impairment
CUI: C1384666
Disease: hearing impairment
337 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2010 2010
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
64 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1 2001 2001
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1 2001 2001
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2002 2002
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 1999 1999
Insulin resistance syndrome
CUI: C3714619
Disease: Insulin resistance syndrome
15 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2005 2005
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2005 2005
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1 2013 2013
Malignant neoplasm of colon and/or rectum
502 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2013 2013
Massive Osteolyses
CUI: C0029438
Disease: Massive Osteolyses
11 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2016 2016
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2018 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2009 2009
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2010 2010
Obesity, Morbid
CUI: C0028756
Disease: Obesity, Morbid
49 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2001 2001
Recurrent depression
CUI: C0221480
Disease: Recurrent depression
12 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2013 2013
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.020 1.000 2 2001 2017